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NCT03080220 · ClinicalTrials.gov registry record · NA

Examining the Effects of Three Soft Tissue Treatments on Functional Movement and Functional Performance Enhancement

A NA study of Functional Performance, sponsored by Rocky Mountain University of Health Professions.

Completed
Registry status
NA
Development phase
48
Enrollment target
3
Study locations

NCT03080220: Completed NA study of Functional Performance, sponsored by Rocky Mountain University of Health Professions.

NCT03080220 is a NA study of Functional Performance that has completed, run by Rocky Mountain University of Health Professions. The registered enrollment target is 48 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). The trial reports 3 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03080220, a NA study of Functional Performance, has completed, sponsored by Rocky Mountain University of Health Professions.

COMPLETED
Registry status
NA
Development phase
48 participants
Enrollment target
3
Study locations

Study Summary

The purpose of this study is to investigate the effects of Astym® treatment, The Stick® treatment and massage treatment on performance among healthy college athletes and to investigate any relationship between functional movement and functional performance. Participants will be recruited from Division II, National Association of Intercollegiate Athletics (NAIA) basketball and volleyball teams. The participants will be randomized into one of three groups: Astym treatment (AT), The Stick treatment (ST) or massage treatment (MT). The participant will have baseline measures of vertical jump (VJ), Y-Balance Lower Quarter Screen (YBLQ), and a rating of current perceived lower extremity function using a visual analog scale (PLEF-VAS). The participants will be treated using either the AT, ST, or MT following baseline measures. Immediately following the intervention, a second measurement of VJ, YBLQ, and PLEF-VAS will take place. The data will be analyzed using mixed ANOVA tests which will be conducted for each dependent variable. In addition, functional movement is thought to be related to functional performance. A Pearson Product Correlation analysis will be used to understand any relationship between YBLQ and VJ. It is hypothesized that those in the AT group will have different percent change in their YBLQ, VJ, and PLEF-VAS compared to those in ST and MT groups. It is hypothesized that a correlation between YBLQ and VJ will exist. As a result, clinicians could use AT among basketball and volleyball athletes without hindering acute performance. Any risks the participants could encounter are minimal. Participants may withdraw themselves and their data at any time. The intervention and testing are similar to what an athlete would be exposed to during their collegiate career. Any participant injured during this study will be referred to their university sports medicine staff, health center, or the Indiana Wesleyan University health center.

Primary Outcome

A Belt Mat (University of Toronto; Toronto, Canada) vertical jump measuring device will be utilized for this study.28

Conditions Studied

Interventions

  • DEVICE Astym
  • DEVICE Stick
  • DEVICE Massage

Study Locations (3)

Indiana

  • University of Saint Francis - Fort Wayne
  • Huntington University - Huntington
  • Indiana Wesleyan University - Marion

Trial Details

FieldValue
Enrollment Target 48 participants
Start Date 2016-09-01
Est. Completion 2016-09-30
Phase NA

What the finished NCT03080220 record still lists

NCT03080220 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 48 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).

The record links to 1 condition, with Functional Performance appearing as the primary indexed condition, and to 3 interventions - of which Astym is the first listed.

NCT03080220 reports a single indexed study location in Indiana.

Frequently Asked Questions

What is clinical trial NCT03080220 about?

NCT03080220 is a clinical study titled "Examining the Effects of Three Soft Tissue Treatments on Functional Movement and Functional Performance Enhancement". The purpose of this study is to investigate the effects of Astym® treatment, The Stick® treatment and massage treatment on performance among healthy college athletes and to investigate any relationship between functional movement and functional performance. Participants will be recruited from Divisi...

What is the current status of trial NCT03080220?

This trial is currently completed. It is a NA study. The enrollment target is 48 participants. The study started on 2016-09-01. Estimated completion is 2016-09-30.

What conditions does trial NCT03080220 study?

This clinical trial studies the following conditions: Functional Performance.

What interventions are being tested in trial NCT03080220?

The interventions under investigation include: Astym (DEVICE), Stick (DEVICE), Massage (DEVICE).

Who is sponsoring clinical trial NCT03080220?

This trial is sponsored by Rocky Mountain University of Health Professions, which has 2 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03080220 being conducted?

This trial has 3 study locations across Indiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

How this trial's enrollment target compares

Where NCT03080220's enrollment target sits among peer trials

48 1381st of 2000 higher than 601 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03080220, the US trial registry maintained by the National Library of Medicine. NCT03080220 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.